For research use only
| Cat No. | ABC-KH005Y |
| Product Type | Knockout Stable Cell Line |
| Cell Type | Monocyte |
| Species | Human |
| Host Cell | THP-1 |
| Source Organ | Peripheral Blood |
| Disease | Acute Monocytic Leukemia |
| Storage | Liquid Nitrogen |
FCGR1A (CD64) knockout THP-1 cell line by AcceGen enables precise study of antibody-dependent phagocytosis and Fc receptor-mediated immune responses.
The FCGR1A (CD64) Knockout THP-1 Cell Line is a CRISPR/Cas9-engineered human monocytic model derived from THP-1 cells, featuring targeted disruption of the Fc gamma receptor Ia (FcγRI/CD64) gene. This high-affinity IgG receptor is a key mediator of antibody-dependent cellular phagocytosis (ADCP) and immune complex clearance. Loss of CD64 expression results in impaired Fcγ receptor signaling, while the cells retain hallmark THP-1 properties including suspension growth, round morphology, and PMA-induced differentiation capacity. This knockout system provides a powerful tool for mechanistic studies of Fc receptor function, autoimmune disease modeling, and evaluation of therapeutic antibody efficacy. Maintained at low passage numbers (<P20) to ensure genetic stability, the knockout is validated by genomic PCR, sequencing, and flow cytometry. Each batch is rigorously tested to confirm absence of HIV-1, HBV, HCV, syphilis, mycoplasma, fungi, yeast, and bacteria.
| Species | Human |
| Cat.No | ABC-KH005Y |
| Product Category | Transfected Stable Cell Lines |
| Size/Quantity | 1 vial |
| Cell Type | Monocyte |
| Growth Mode | Suspension |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Peripheral Blood |
| Disease | Acute Monocytic Leukemia |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Knockout Stable Cell Line |
| Host Cell | THP-1 |
| Gene Info | CD64 |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
The FCGR1A (CD64) Knockout THP-1 Cell Line is a genetically engineered human monocyte model with targeted disruption of the high-affinity IgG Fc receptor gene. This modification eliminates surface CD64 expression, creating a specialized tool for investigating antibody-dependent cellular phagocytosis (ADCP), immune complex clearance, and Fc receptor signaling pathways. The cell line enables precise mechanistic studies of therapeutic antibody function and FcγR-mediated immune responses while retaining monocyte differentiation capacity.